510(k) K063723 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
IMPELLA RECOVER LP 2.5 PERCUTANEOUS CARDIAC SUPPORT SYSTEM
| Applicant | Abiomed, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, May 30, 2008 |
| Received | Dec 15, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063723
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.